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Items: 1 to 20 of 237

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7065964inversion1nstd229human GRCh38 chr13: 92,033,887-93,656,929 , GRCh37.p13 chr13: 92,686,140-94,309,182 GPC5-AS2, GPC5, 9 more genes
    nsv6957565copy number variation1nstd229human GRCh38 chr13: 93,051,167-93,055,493 , GRCh37.p13 chr13: 93,703,420-93,707,746 LINC00363
    nsv6956892copy number variation1nstd229human GRCh38 chr13: 92,644,056-93,213,917 , GRCh37.p13 chr13: 93,296,309-93,866,170 LOC105370317, GPC5-AS1, 3 more genes
    nsv6947856copy number variation1nstd229human GRCh38 chr13: 91,420,012-93,527,013 , GRCh37.p13 chr13: 92,072,266-94,179,266 GPC6, LOC105370315, 9 more genes
    nsv6946189copy number variation1nstd229human GRCh38 chr13: 93,038,201-93,058,800 , GRCh37.p13 chr13: 93,690,454-93,711,053 LINC00363
    nsv6940509copy number variation1nstd229human GRCh38 chr13: 93,045,034-93,058,759 , GRCh37.p13 chr13: 93,697,287-93,711,012 LINC00363
    nsv6940467copy number variation1nstd229human GRCh38 chr13: 93,050,521-93,073,357 , GRCh37.p13 chr13: 93,702,774-93,725,610 LINC00363
    nsv6939951copy number variation1nstd229human GRCh38 chr13: 92,865,201-93,092,300 , GRCh37.p13 chr13: 93,517,454-93,744,553 LOC105370317, GPC5, 1 more genes
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637762copy number variation1nstd102humanUncertain significance GRCh37 chr13: 92,072,602-94,178,694 , GRCh38.p12 chr13: 91,420,348-93,526,441 GPC5-AS1, HNRNPA1P29, 9 more genes
    nsv6637615copy number variation1nstd102humanPathogenic GRCh37 chr13: 93,535,335-105,788,229 , GRCh38.p12 chr13: 92,883,082-105,135,878 SNORD13G, FTLP8, 162 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6483886copy number variation1nstd223human GRCh38 chr13: 92,644,056-93,213,914 , GRCh37.p13 chr13: 93,296,309-93,866,167 LINC00363, GPC5, 3 more genes
    nsv6315552copy number variation1nstd102humanPathogenic GRCh37 chr13: 89,490,345-115,062,235 , GRCh38.p12 chr13: 88,838,091-114,296,760 MIR20A, MIR548AR, 347 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314171copy number variation1nstd102humanPathogenic GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258 MIR4705, LOC102724149, 430 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6313971copy number variation1nstd102humanPathogenic GRCh37 chr13: 85,037,147-115,107,733 , GRCh38.p12 chr13: 84,463,012-114,342,258 BRK1P2, UGGT2, 386 more genes
    nsv6313904copy number variation1nstd102humanPathogenic GRCh37 chr13: 78,514,567-115,107,733 , GRCh38.p12 chr13: 77,940,432-114,342,258 LOC101927284, LOC105370330, 444 more genes
    nsv6291741copy number variation1nstd102humanLikely benign GRCh37 chr13: 93,296,805-93,862,088 , GRCh38.p12 chr13: 92,644,552-93,209,835 GPC5-AS1, LOC105370315, 3 more genes
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